Characterisation of the

Background: Mentha canadensis L. has important economic value for the production of essential oils, which are synthesised, secreted and stored in peltate glandular trichomes. As a typical multicellular secretory trichome, glandular trichomes are important biological factories for the synthesis of some specialised metabolites. However, little is known about the molecular mechanism of glandular trichome development in M. canadensis. Results: In this study, the R2R3-MYB transcription factor gene McMIXTA was isolated to investigate its function in glandular trichome development. Bioinformatics analysis indicated that McMIXTA belonged to the subgroup 9 R2R3MYB, with a R2R3 DNA-binding domain and conserved subgroup 9 motifs. A subcellular localisation assay indicated that McMIXTA was localised in the nucleus. Transactivation analysis indicated that McMIXTA was a positive regulator, with transactivation regions located between positions N253 and N307. Yeast two-hybrid and bimolecular fluorescence complementation assays showed that McMIXTA formed a complex with McHD-Zip3, a trichome developmentrelated HD-ZIP IV transcription factor. Overexpression of McMIXTA in Mentha × piperita L. caused an increase in peltate glandular trichomes density of approximately 25% on the leaf abaxial surface. Conclusions: Our results demonstrated that the subgroup 9 R2R3-MYB transcription factor McMIXTA has a positive effect on regulating peltate glandular trichome development and the MIXTA/HD-ZIP IV complexes might be conserved regulators for glandular trichome initiation. These results provide useful information for revealing the regulatory mechanism of multicellular glandular trichome development. Keyword: Mentha canadensis L.; Glandular trichome; McMIXTA; McHD-Zip3 © The Author(s) 2022. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http:// creat iveco mmons. org/ licen ses/ by/4. 0/. The Creative Commons Public Domain Dedication waiver (http:// creat iveco mmons. org/ publi cdoma in/ zero/1. 0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. Background Trichomes are appendages derived from cells of the aerial epidermis, and are found in numerous plant species worldwide [1]. Trichomes vary in size, morphology, cellular composition, and function, and can be categorised into unicellular and multicellular or secretory and non-secretory types according to their cell number and secretory ability [2, 3]. For instance, Arabidopsis thaliana trichomes are unicellular and non-secretory [4]. Secretory or glandular trichomes synthesise or secrete large amounts of specialised metabolites that enhance plant fitness and may also be beneficial for humans [5, 6]. For example, glandular trichomes of Artemisia annua secrete the sesquiterpene metabolite artemisinin, which is an effective anti-malarial drug [7]. Open Access *Correspondence: liangcy618@cnbg.net Xiwu Qi and Zequn Chen are contributed equally to this work. 1 Jiangsu Key Laboratory for the Research and Utilization of Plant Resources, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences, Nanjing 210014, China Full list of author information is available at the end of the article Page 2 of 11 Qi et al. BMC Plant Biology (2022) 22:219 The amounts of metabolites secreted by glandular trichomes are generally correlated to their density [7, 8]. Increased glandular trichome density is considered to be an effective strategy to increase the accumulation of specialised metabolites [7]. Therefore, the genetic networks of glandular trichome development provide an important basis for genetic engineering of glandular trichome. In A. thaliana, more than 70 genes regulating trichome development have been identified and characterised, revealing a complex regulatory network for trichome [9–14]. In contrast to the unicellular trichomes of Arabidopsis, the regulatory networks of multicellular glandular trichome development in other species remain poorly understood [15]. To date, only a few genes regulating multicellular glandular trichome development have been identified, which mainly encode some transcription factors, including MYB, HD-ZIP, C2H2, bHLH and so on [15]. The MIXTA gene, which was first characterised in Antirrhinum majus, encodes one of the most important regulators of glandular trichomes and promotes trichome initiation [16–18]. Homologous genes have also been identified in A. annua and Solanum lycopersicum, which have been shown to have similar functions in promoting glandular trichome initiation [19, 20]. In addition to MIXTA genes, several HD-ZIP IV transcription factors have also been shown to participate in regulating glandular trichome development [15]. For example, AaHD1 and AaHD8 in A. annua can promote the development of glandular trichome [21, 22]. In S. lycopersicum, SlWOOLLY and SlCD2 have been shown to participate in regulation of glandular trichome initiation [23–25]. Further, there is evidence that the glandular trichome-related MIXTA and HD-ZIP transcription factors may function through interaction. In A. annua, AaMIXTA1 and AaHD8 show similar functions in promoting glandular trichome initiation, and they interact to form complexes. The interaction of AaMIXTA1 and AaHD8 produces a much greater effect than their additive effects [22]. In S. lycopersicum, SlMIXTA-like and SlCD2 may also interact to form a co-regulation network [15]. Mentha canadensis L. (Lamiaceae) can produce a large amount of aromatic essential oils, which are widely used in food additives, cosmetics and medical industries [26]. The main components of essential oils are monoterpenoids, which are synthesised, secreted, and stored in glandular trichomes [27, 28]. The biosynthetic pathway of monoterpenoids in essential oils has been extensively studied in the genus Mentha [29–31]. However, the genetic mechanism of the involvement of glandular trichomes in essential oil biosynthesis has rarely been explored. The surface of M. canadensis bears three types of trichomes: non-glandular, capitate glandular, and peltate glandular trichomes; among these, peltate glandular trichomes are the centre of essential oil biosynthesis [32]. In our previous study, we demonstrated that McHDZip3, a HD-Zip IV transcription factor of M. canadensis, participated in promoting glandular trichome development [33]. However, the regulation mechanism of glandular trichome development in M. canadensis requires further study. Therefore, in this study, we cloned the MIXTA homologue gene McMIXTA from M. canadensis and characterised its regulatory role in glandular trichome development. We further examined whether McMIXTA interacted with the HD-ZIP IV transcription factor McHD-Zip3 to form a complex. The results of this study will contribute to elucidating the molecular mechanism of multicellular glandular trichome development in M. canadensis.


Background
Trichomes are appendages derived from cells of the aerial epidermis, and are found in numerous plant species worldwide [1]. Trichomes vary in size, morphology, cellular composition, and function, and can be categorised into unicellular and multicellular or secretory and non-secretory types according to their cell number and secretory ability [2,3]. For instance, Arabidopsis thaliana trichomes are unicellular and non-secretory [4]. Secretory or glandular trichomes synthesise or secrete large amounts of specialised metabolites that enhance plant fitness and may also be beneficial for humans [5,6]. For example, glandular trichomes of Artemisia annua secrete the sesquiterpene metabolite artemisinin, which is an effective anti-malarial drug [7].

Open Access
*Correspondence: liangcy618@cnbg.net † Xiwu Qi and Zequn Chen are contributed equally to this work. 1 Jiangsu Key Laboratory for the Research and Utilization of Plant Resources, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences, Nanjing 210014, China Full list of author information is available at the end of the article The amounts of metabolites secreted by glandular trichomes are generally correlated to their density [7,8]. Increased glandular trichome density is considered to be an effective strategy to increase the accumulation of specialised metabolites [7]. Therefore, the genetic networks of glandular trichome development provide an important basis for genetic engineering of glandular trichome. In A. thaliana, more than 70 genes regulating trichome development have been identified and characterised, revealing a complex regulatory network for trichome [9][10][11][12][13][14]. In contrast to the unicellular trichomes of Arabidopsis, the regulatory networks of multicellular glandular trichome development in other species remain poorly understood [15]. To date, only a few genes regulating multicellular glandular trichome development have been identified, which mainly encode some transcription factors, including MYB, HD-ZIP, C2H2, bHLH and so on [15]. The MIXTA gene, which was first characterised in Antirrhinum majus, encodes one of the most important regulators of glandular trichomes and promotes trichome initiation [16][17][18]. Homologous genes have also been identified in A. annua and Solanum lycopersicum, which have been shown to have similar functions in promoting glandular trichome initiation [19,20].
In addition to MIXTA genes, several HD-ZIP IV transcription factors have also been shown to participate in regulating glandular trichome development [15]. For example, AaHD1 and AaHD8 in A. annua can promote the development of glandular trichome [21,22]. In S. lycopersicum, SlWOOLLY and SlCD2 have been shown to participate in regulation of glandular trichome initiation [23][24][25]. Further, there is evidence that the glandular trichome-related MIXTA and HD-ZIP transcription factors may function through interaction. In A. annua, AaMIXTA1 and AaHD8 show similar functions in promoting glandular trichome initiation, and they interact to form complexes. The interaction of AaMIXTA1 and AaHD8 produces a much greater effect than their additive effects [22]. In S. lycopersicum, SlMIXTA-like and SlCD2 may also interact to form a co-regulation network [15].
Mentha canadensis L. (Lamiaceae) can produce a large amount of aromatic essential oils, which are widely used in food additives, cosmetics and medical industries [26]. The main components of essential oils are monoterpenoids, which are synthesised, secreted, and stored in glandular trichomes [27,28]. The biosynthetic pathway of monoterpenoids in essential oils has been extensively studied in the genus Mentha [29][30][31]. However, the genetic mechanism of the involvement of glandular trichomes in essential oil biosynthesis has rarely been explored. The surface of M. canadensis bears three types of trichomes: non-glandular, capitate glandular, and peltate glandular trichomes; among these, peltate glandular trichomes are the centre of essential oil biosynthesis [32]. In our previous study, we demonstrated that McHD-Zip3, a HD-Zip IV transcription factor of M. canadensis, participated in promoting glandular trichome development [33]. However, the regulation mechanism of glandular trichome development in M. canadensis requires further study.
Therefore, in this study, we cloned the MIXTA homologue gene McMIXTA from M. canadensis and characterised its regulatory role in glandular trichome development. We further examined whether McMIXTA interacted with the HD-ZIP IV transcription factor McHD-Zip3 to form a complex. The results of this study will contribute to elucidating the molecular mechanism of multicellular glandular trichome development in M. canadensis.

McMIXTA is a subgroup 9 R2R3-MYB transcription factor in M. canadensis
In this study, we isolated the homologous gene of MIXTA in M. canadensis, which we named McMIXTA (Gen-Bank accession number: OL624641). Phylogenetic analysis showed that McMIXTA was clustered into one clade with other subgroup 9 MYB members, most of which have been characterised as regulators associated with epidermal cell differentiation (Fig. 1). A comparison of the CDS and corresponding genome sequence showed that McMIXTA contained four exons and three introns ( Fig. 2A). The CDS of McMIXTA was 1137 bp in length, which encoded a 337 amino acid protein with a theoretical molecular weight of 40.7 kDa and a theoretical isoelectric point of 5.97. Multi-sequence alignment showed that McMIXTA shared a conserved R2R3 repeat region and subgroup 9-specific motifs SG9 and SG9-A with other subgroup 9 R2R3-MYBs (Fig. 2B). These results suggest that McMIXTA is a subgroup 9 R2R3-MYB transcription factor in M. canadensis.

McMIXTA is a nuclear-localised protein
Transcription factors mainly perform regulatory functions in the nucleus. In this study, Agrobacterium-mediated transient transformation in Nicotiana benthamiana epidermal cells was conducted to analyse the subcellular localisation of McMIXTA. Using fusion-expressed GFP as a marker, we found that the McMIXTA-GFP fusion protein was present only in the nucleus, whereas GFP was present in the whole cell (Fig. 3). These results suggest that McMIXTA is localised in the nucleus.

The McMIXTA N253-307 region is sufficient for transactivation
Yeast cells were used to identify the transactivation region of McMIXTA. The full-length CDS and a series of C-terminal truncated CDSs of McMIXTA were fused separately to the GAL4 DNA BD in pGBKT7 vector and transformed into yeast strain AH109. Screening medium and a LacZ activity assay were used to detect the transactivation activity of the recombinant plasmids.
The results showed that three forms of McMIXTA with amino acid length > 307 (M1 Full length, M2 ΔN343-378, and M3 ΔN308-378), had transcriptional activation activity, whereas the other three forms with amino acid length < 252 (M4 ΔN253-278, M5 ΔN196-378, and M6 ΔN129-378) did not (Fig. 4), suggesting that the transcriptional activation regions of McMIXTA may be located between N253 and N307. To confirm whether the region between positions N253 and N307 of McMIXTA was sufficient for transactivation, these regions were cloned into the pGBKT7 vector and assayed using yeast cells. The results indicate that region N253-307 of McMIXTA is sufficient for transactivation (Fig. 4).

Overexpression of McMIXTA promotes peltate glandular trichome initiation in M. piperita
To determine whether McMIXTA has an effect on peltate glandular trichome initiation in mint plants,   (Fig. 5A, B). Due to the small field of SEM, we further used stereo fluorescence microscopy to count the number of peltate glandular trichomes on leaves, in order to obtain more accurate data. Because peltate glandular trichomes are not evenly distributed on leaves, we obtained images of three relatively fixed visual fields per leaf to represent the average peltate glandular trichome density of the leaf (Fig. 5C). Peltate glandular trichome count results showed that the density of peltate glandular trichome decreased gradually with the growth of leaves (Fig. 5E). Comparing transgenic plants with wild-type plants showed that the second, third, and fourth leaves of McMIXTA overexpressed transgenic plants had significantly higher peltate glandular trichome density than those of the WT and the increase in peltate glandular trichome density was about 25% (Fig. 5D, E). These results suggest that overexpression of McMIXTA promotes the initiation of peltate glandular trichomes in M. piperita.

McMIXTA interacted with the glandular trichome development-related transcription factor McHD-Zip3
Studies have shown that MIXTA interacts with HD-ZIP IV transcription factors to form complexes that regulate epidermal cell development [15,22]. In our previous study, we identified the HD-ZIP IV transcription factor McHD-Zip3 in M. canadensis, which promoted glandular trichome development [33]. Therefore, we attempted to detect an interaction between McMIXTA and McHD-Zip3 in this study. Due to strong transcriptional self-activation of McMIXTA, we performed a deletion analysis; we found that the AD was localised in residues 252-307 at the C-terminus. Consequently, M4, M5, and M6 were fused to the yeast GAL4 BD and McHD-Zip3 was fused to the yeast GAL4 AD. Results of a Y2H assay showed that M4 interacted with McHD-Zip3, but M5 and M6 did not (Fig. 6A) [35] and AtMYB2 is located in amino acids 221-274 (of 274) [36]. However, the transactivation region of AtMYB12 is not located at the rearmost C-terminal end but rather near the C-terminus (amino acids 273-325, of 371) [37]. Our results showed that the transactivation region of McMIXTA is located in amino acids 253-307 (of 378), which is farther from the C-terminal end than those of previously reported R2R3-MYB transcription factors. Although the location is different, the transactivation region of McMIXTA is rich in acidic amino acids, which is consistent with other R2R3-MYB transcription factors [35][36][37].
R2R3-MYB transcription factors represent a large gene family that can be divided into more than 22 subgroups according to the conservation motifs of the C-terminal [34,38]. Several subgroup 9 R2R3-MYB transcription factors have been shown to regulate epidermal cell differentiation. In Arabidopsis, AtMYB16 and AtMYB106 (subgroup 9) have been shown to function in controlling epidermal regulation and trichome branch formation [39,40]. AaMIXTA1 is a subgroup 9 R2R3-MYB that positively regulates glandular trichome initiation in A. annua [19]. In S. lycopersicum, two subgroup 9 R2R3-MYBs, SlMX1 and SlMIXTA-like, also participate in regulating trichome development [20,41]. GhMYB25 and GhMYB25-like (Subgroup 9) regulate the initiation and timing of initial fibre expansion in cotton [42,43]. In this study, McMIXTA overexpression resulted in higher glandular trichomes density in M. piperita, indicating that McMIXTA functions similarly in the regulation of trichome development to other subgroup 9 homologues. However, different types of trichomes have different transcriptional regulatory patterns. For example, the MIXTA gene in A. majus promotes the development of multicellular glandular trichomes in N. benthamiana, but has no effect on unicellular trichomes in Arabidopsis [44]. In contrast, Arabidopsis AtMYB16 regulates the development of unicellular trichomes but has no effect on multicellular trichomes [39]. These results suggest that although the functions of subgroup 9 members are conserved to Studies have shown that MIXTA interacts with HD-ZIP IV transcription factors to form complexes that regulate epidermal cell development. In cotton, the MIXTA-like transcription factor GhMYB25 and HD-ZIP IV transcription factor GhHD1 interact with each other, and both have a positive effect on regulating trichome initiation in fibres [45]. In A. annua, AaMX-ITA1 and AaHD8 have similar functions in the positive regulation of glandular trichome initiation, and interact with each other to form complexes. In S. lycopersicum, a co-regulation network between SlMIXTA-like and SlCD2 may also be formed through interaction [15]. In the present study, we also found that McMIXTA interacted with the HD-ZIP IV transcription factor McHD-Zip3 and both of them functions in regulating glandular trichome development [33]. However, the effect of the interaction between MIXTA and HD-ZIP IV on glandular trichome development is rarely reported. In A. annua, the activation of AaHD8 to target promoters was significantly enhanced by AaMIXTA1, similarly, the activation of AaMIXTA1 to target promoters was also enhanced by AaHD8, and the enhancement was more than addition of their individual promotion. However, whether this enhancement on target genes can promote more glandular trichomes remains unclear [22]. The interaction between MIXTA and HD-Zip IV transcription factors on glandular trichome development still needs further study. In this study, we demonstrated that N195-252 of McMIXTA may be the key region binding to McHD-Zip3, which is consistent with the AaMIXTA1 in A. annua. The C-terminal region of AaMIXTA1 is required for its interaction with AaHD8, whereas the R2R3 domain is not needed. Together, it is possible that MIXTA/HD-ZIP IV complexes are conserved regulators of epidermal cell development in plants and play major roles in trichome initiation.

Plant materials
The M. canadensis and Mentha × piperita L. plants used in this study were maintained at the Germplasm Nursery at the Institute of Botany, Jiangsu Province and the Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing, Jiangsu Province. Leaves of M. canadensis were collected and stored at − 80 °C until further use. N. benthamiana plants were cultured in an artificial climate chamber (Jiangnan, Ningbo, China) at 25 °C under a 14-h light/10-h dark cycle (120 μmol/m 2 /s).

RNA isolation and cDNA synthesis
Total RNA of M. canadensis and M. piperita samples was extracted using the FastPure Plant Total RNA Isolation Kit (Vazyme, Nanjing, China) according to the manufacturer's instructions. RNA quality and concentration were measured using a NanoDrop 2000 spectrophotometer (Thermo Scientific, Waltham, MA, USA). Next, 1 μg of RNA was used to synthesise first-strand cDNA using the HiScript II 1st Strand cDNA Synthesis Kit (Vazyme).

Isolation and characterisation of McMIXTA
The candidate gene McMIXTA was isolated by polymerase chain reaction (PCR) amplification using M. canadensis cDNA as template and primers listed in Table 1. The PCR products were separated by gel electrophoresis and the target fragments were purified and cloned using the 5 min TA/Blunt-Zero Cloning Kit (Vazyme). Positive clones were screened and sequenced by Sangon Biotech (Shanghai) Co., Ltd. for confirmation. The deduced amino acid sequence and corresponding theoretical molecular weights and isoelectric points of McMIXTA were predicted in ExPASy (https:// www. expasy. org/) [46]. Muscle3.6 was used to conduct the multiple sequence alignment [47]. The neighbour-joining phylogenetic tree was constructed using MEGA4 software with bootstrap testing of 1,000 replications [48]. The bootstrap consensus tree was exported in the Newick file format and modified using the EvolView online tool (https:// www. evolg enius. info// evolv iew/# login) [49].

Subcellular localisation assay of McMIXTA
For subcellular localisation assay, coding sequences (CDSs) of McMIXTA were amplified and cloned into the p35SGK-GFP vector using the ClonExpress II One Step Cloning Kit (Vazyme). Primer sequences were listed in Table 1. The recombinant plasmid was transformed into Agrobacterium tumefaciens strain EHA105, and the p35SGK-GFP vector without McMIXTA was transformed into A. tumefaciens strain EHA105 as a control. Transient transformation was conducted by infiltrating N. benthamiana leaves with A. tumefaciens strain EHA105 expressing McMIXTA-GFP or GFP only. After 48 h, a laser confocal microscope (Zeiss, Oberkochen, Germany) was used to observe the GFP signals.

Transactivation activity analysis of McMIXTA
The transactivation activity of McMIXTA was analysed in yeast cells as previously described [50]. To determine the transcriptional activation region of McMIXTA, the full-length CDS of McMIXTA and a series of C-terminal truncated CDSs of McMIXTA were cloned into the pGBKT7 vector (Clontech). The recombinant plasmids were transformed into yeast strain AH109 and cultured on SD/-Trp medium. Then, the yeast cells were further screened on SD/-Trp or SD/-Trp/-His/-Ade plus 3-AT medium. LacZ activity was assayed by adding X-α-gal to the medium. After the transactivation regions were screened, the identified regions were cloned into the pGBKT7 vector; the yeast assay was also used to detect independent transactivation activity. Primers used for vector construction are listed in Table 1.

Yeast two-hybrid (Y2H) assay
For the Y2H assay, the CDS of McHD-Zip3 was amplified and cloned into pGADT7 to generate the GAL4 activation domain (AD) vector using primers listed in Table 1. pGBKT7 inserted with full-length or truncated CDSs of McMIXTA was used as the GAL4 BD vector. The Y2H assay was conducted by co-transformation of the AD and BD vectors to yeast strain AH109 and cultured on SD/-Trp/-Leu medium. Then, the yeast cells were screened on SD/-Trp/-Leu or SD/-Ade/-His/-Leu/-Trp medium. X-αgal was added to the medium to detect the activity of the reporter gene MEL1.

Bimolecular fluorescence complementation (BiFC) assay
The pXY103 and pXY105 vectors containing N-terminal and C-terminal CDSs of yellow fluorescent protein (YFP) were used for the BiFC assay. CDSs of McHD-Zip3 and McMIXTA were fused to the N-terminal and C-terminal of YFP, respectively, using primers listed in Table 1. The recombinant vectors were transformed into A. tumefaciens strain EHA105. After A. tumefaciens culturing, different combinations of nYFP and cYFP bacterial solutions were co-infiltrated into N. benthamiana leaves. After 48 h, the fluorescence signals were observed using a laser confocal microscope (Zeiss).

Genetic transformation of M. piperita
CDSs of McMIXTA were cloned into the plant binary expression vector p35SGK using the ClonExpress II One Step Cloning Kit (Vazyme) using primers listed in Table 1. The expression of the inserted gene was controlled by the CaMV 35S promoter. The recombinant plasmid was transformed into A. tumefaciens EHA105 competent cells. Transformation of M. piperita was conducted as previously described [51], with some modification. Briefly, sterile stems were used as explants and pre-cultured on pre-culture medium for 2 days. Then, the explants were submerged in A. tumefaciens containing the recombinant plasmid p35SGK-McMIXTA and incubated for 20 min with gentle shaking. The explants were dried with sterilised blotting paper and cultured in co-cultivation medium for 2 days in the dark. Then, the explants were transferred to screening medium containing 50 mg/L kanamycin and 25 mg/L rifampicin and  cultured at 25 °C under a 16-h light/8-h dark cycle. After 6 weeks, resistant plants differentiated from explants on the screening medium were transferred to rooting medium. Well-rooted plants were then transferred to vegetative soil for culture.

Scanning electron microscopy (SEM)
The peltate glandular trichomes of transgenic and wildtype (WT) M. piperita were observed using scanning electron microscopy. For sample preparation, the second leaves were fixed overnight in 2.5% glutaraldehyde prepared in 0.1 M potassium phosphate buffer. Then the samples were washed with distilled water and dehydrated in an ethanol and acetone series. After dehydration, the samples were critical point dried and fixed on spherical metal stubs. The abaxial surface of leaves was coated with a thin layer of gold and observed using FEI Quanta 200 scanning electron microscope (FEI, Hillsboro, USA).

Peltate glandular trichome density counts
The second, third, and fourth leaves of transgenic and WT M. piperita were used to determine peltate glandular trichome density. Peltate glandular trichomes on the leaf abaxial surface were observed under a stereo fluorescence microscope (Olympus, Tokyo, Japan) with a × 5 objective at an excitation wavelength of 480 nm. The peltate glandular trichome number was determined using the ImageJ software. Because peltate glandular trichomes are not evenly distributed on leaves, we obtained images for three relatively fixed visual fields per leaf to represent the average peltate glandular trichome density of the leaf. The leaves of six plants were measured for both transgenic and WT lines. We declare that all methods were carried out in accordance with relevant guidelines and regulations